(1R,2E,5E,9E)-3,7,7,10-tetramethylcycloundeca-2,5,9-trien-1-ol

Details

Top
Internal ID 8b3c5ce3-6568-4659-905f-e6569bbca05b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,2E,5E,9E)-3,7,7,10-tetramethylcycloundeca-2,5,9-trien-1-ol
SMILES (Canonical) CC1=CC(CC(=CCC(C=CC1)(C)C)C)O
SMILES (Isomeric) C/C/1=C\[C@@H](C/C(=C/CC(/C=C/C1)(C)C)/C)O
InChI InChI=1S/C15H24O/c1-12-6-5-8-15(3,4)9-7-13(2)11-14(16)10-12/h5,7-8,10,14,16H,6,9,11H2,1-4H3/b8-5+,12-10+,13-7+/t14-/m0/s1
InChI Key KPNGOCXLTVWHAC-GETKEXHGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.40
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (1R,2E,5E,9E)-3,7,7,10-tetramethylcycloundeca-2,5,9-trien-1-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.9267 92.67%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.5124 51.24%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.9329 93.29%
OATP1B3 inhibitior + 0.9692 96.92%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5608 56.08%
P-glycoprotein inhibitior - 0.9390 93.90%
P-glycoprotein substrate - 0.8890 88.90%
CYP3A4 substrate + 0.5085 50.85%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7543 75.43%
CYP3A4 inhibition - 0.8369 83.69%
CYP2C9 inhibition - 0.7791 77.91%
CYP2C19 inhibition - 0.6962 69.62%
CYP2D6 inhibition - 0.9369 93.69%
CYP1A2 inhibition - 0.7722 77.22%
CYP2C8 inhibition - 0.9192 91.92%
CYP inhibitory promiscuity - 0.8758 87.58%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7252 72.52%
Carcinogenicity (trinary) Non-required 0.5941 59.41%
Eye corrosion - 0.9065 90.65%
Eye irritation + 0.7895 78.95%
Skin irritation + 0.7257 72.57%
Skin corrosion - 0.9067 90.67%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4794 47.94%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6700 67.00%
skin sensitisation + 0.7706 77.06%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.7203 72.03%
Acute Oral Toxicity (c) III 0.7909 79.09%
Estrogen receptor binding - 0.8957 89.57%
Androgen receptor binding - 0.9001 90.01%
Thyroid receptor binding - 0.7542 75.42%
Glucocorticoid receptor binding - 0.7418 74.18%
Aromatase binding - 0.6332 63.32%
PPAR gamma - 0.6885 68.85%
Honey bee toxicity - 0.9093 90.93%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9301 93.01%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.44% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.89% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 86.97% 97.79%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.97% 86.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.45% 97.25%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Betula pendula

Cross-Links

Top
PubChem 162990418
LOTUS LTS0239494
wikiData Q105144289